HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → Ethyl 2-phenylsulfanyl-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromothiazole-5-carboxylate | HCID 3614103 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-phenylsulfanyl-thiazole-5-carboxylate | HCID 10901519 | 48% |
Reaction Steps
A suspension of 2-bromo-1,3-thiazole-5-carboxylic acid ethyl ester (1.5 g, 6.15 mmol, 1 eq) and K2CO3 (1.7 g, 12.3 mmol, 2 eq) in EtOH (60 mL) is cooled in an ice bath, and thiophenol (0.631 mL, 6.15 mmol, 1 eq) is added. The reaction is monitored by HPLC until the starting material is consumed. The reaction mixture is filtered (to remove a solid by-product), and the solvent is removed in vacuo. The crude mixture is purified by silica gel chromatography using a Biotage Flash 40S column using 2% EtOAc in hexanes to afford the product as an oil (0.784 g, 46%). MS (ESI) for C12H11NO2S2m/z 266.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492385B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-a30e3ab6e8c841d6ba24668fe2cdf3d3 |
| Source note | uspto-grants-2002_12 |